Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.
- NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.
- NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_assertion evidence source_evidence_literature NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.
- NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_assertion SIO_000772 8895241 NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.
- NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_assertion wasDerivedFrom befree-2016 NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.
- NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_assertion wasGeneratedBy ECO_0000203 NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.